摘要
三氮唑是一类重要的有机化合物.本文用点击化学合成了1,4-二取代-1,2,3-三氮唑衍生物.在微波辅助下,碘化亚铜催化叠氮化钠、炔烃、苯磺酸酯三组分反应合成了一系列1,4-二取代-1,2,3-三氮唑衍生物.控制微波功率65~80W,温度50~75℃,反应在15min内完成,产率81%~94%.新化合物结构用红外、1 H-NMR、13 C-NMR、DEPT、HR-MS、元素分析鉴定.实验结果表明该方法条件温和,操作简单,对环境友好.
Triazole is an important organic compound. In this article, we synthesised 1, 4-disubstituted-1,2, 3-triazole derivatives with click chemistry. A microwave-assisted three-component reaction was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from corresponding sodium azide, alkynes and benzene sulfonates via CuI catalyzed. Controling microwave power 65-80 W, temperature 50-75℃, the reaction was completed in 15 min, the yield of 81-94%. The structure of new products(e-p) was confirmed by IR.^1H NMR.^13C NMR.DEPT.HR-MS.elementary analysis. The results indicated that the reaction simple and under mild conditions, and it was environmentally friendly.
出处
《华中师范大学学报(自然科学版)》
CAS
CSCD
北大核心
2011年第3期421-425,共5页
Journal of Central China Normal University:Natural Sciences
基金
江西省高校重点实验室科技计划项目(赣财教GJJ[2007]431)